Epigenetic mark sequence of the H19 gene in human sperm

Biochimica et Biophysica Acta - Gene Structure and Expression

Volumn 1518, Issue 1-2, 2001, Pages 137-144

  Hamatani, Toshio ^a   Sasaki, Hiroyuki ^b   Ishihara, Ko ^b   Hida, Naoko ^a   Maruyama, Tetsuo ^a   Yoshimura, Yasunori ^a   Hata, Jun ichi ^a   Umezawa, Akihiro ^a  

^a KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b GRADUATE UNIVERSITY FOR ADVANCED STUDIES   (Japan)

Author keywords

Bisulfite; H19; Human; Imprinting; Methylation; Sperm

Indexed keywords

CYTOSINE; DINUCLEOTIDE; DNA;

ADULT; ALLELE; ARTICLE; BRAIN; CONTROLLED STUDY; CPG ISLAND; DNA SEQUENCE; GENE EXPRESSION; GENOME IMPRINTING; HUMAN; HUMAN TISSUE; KIDNEY; MALE; METHYLATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROMOTER REGION; SEQUENCE ANALYSIS; SPERM;

ADULT; ANIMALS; BASE SEQUENCE; CPG ISLANDS; DNA METHYLATION; GENES; GENOMIC IMPRINTING; HUMANS; MALE; MICE; MOLECULAR SEQUENCE DATA; PROTEINS; RATS; RNA, UNTRANSLATED; SPERMATOZOA;

EID: 0035911697     PISSN: 01674781     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0167-4781(01)00190-7     Document Type: Article

References (30)

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2. Parental genomic imprinting of the human IGF2 gene
3. Parental imprinting of the mouse H19 gene
4. Imprinting of human H19: Allele-specific CpG methylation, loss of the active allele in Wilms tumor and potential for somatic allele switching
5. Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor
6. The paternal methylation imprint of the mouse H19 locus is acquired in the gonocyte stage during foetal testis development
7. Characterization of novel parent-specific epigenetic modifications upstream of the imprinted mouse H19 gene
8. Chromatin conformation of the H19 epigenetic mark
9. A paternal-specific methylation imprint marks the alleles of the mouse H19 gene
10. A 5′ 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development
11. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2
12. Location of enhancers is essential for the imprinting of H19 and Igf2 genes
13. Enhancer competition between H19 and Igf2 does not mediate their imprinting
14. Role of a 461-bp G-rich repetitive element in H19 transgene imprinting
15. Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus
16. A potential imprint control element: Identification of a conserved 42 bp sequence upstream of H19
17. Comparative genomic sequencing identifies novel tissue-specific enhancers and sequence elements for methylation-sensitive factors implicated in Igf2/H19 imprinting
18. Parental allele-specific chromatin configuration in a boundary-imprinting-control element upstream of the mouse H19 gene
19. CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus
20. Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
21. The 5′ flank of mouse H19 in an unusual chromatin conformation unidirectionally blocks enhancer-promoter communication
22. Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function
23. The protein CTCF is required for the enhancer blocking activity of vertebrate insulators
24. Purification of human sperm by a discontinuous Percoll density gradient with an inner column
25. A method for collecting motile spermatozoa from human semen
26. Methylation of an ETS site in the intron enhancer of the keratin 18 gene participates in tissue-specific repression
27. High sensitivity mapping of methylated cytosines
28. Asymmetric methylation in the hypermethylated CpG promoter region of the human L1 retrotransposon
29. Temporal and spatial regulation of H19 imprinting in normal and uniparental mouse embryos